Name

trong>Severetrong> trong>combinedtrong> trong>immunodeficiency,trong> trong>autosomaltrong> trong>recessive,trong> T cell-negative, B cell-positive, NK cell-positive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Severetrong> trong>combinedtrong> trong>immunodeficiency,trong> trong>autosomaltrong> trong>recessive,trong> T cell-negative, B cell-positive, NK cell-positive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Severetrong> trong>combinedtrong> trong>immunodeficiency,trong> trong>autosomaltrong> trong>recessive,trong> T cell-negative, B cell-positive, NK cell-negative Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Severetrong> trong>combinedtrong> trong>immunodeficiency,trong> trong>autosomaltrong> trong>recessive,trong> T cell-negative, B cell-positive, NK cell-negative phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Severetrong> trong>Combinedtrong> trong>Immunodeficiency,trong> trong>Autosomaltrong> trong>Recessive,trong> T Cell-Negative, B Cell-Positive, NK Cell-Negative Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease trong>Severetrong> trong>Combinedtrong> trong>Immunodeficiency,trong> trong>Autosomaltrong> trong>Recessive,trong> T Cell-Negative, B Cell-Positive, NK Cell-Negative from the curated CTD Gene-Disease Associations dataset.

trong>Severetrong> trong>Combinedtrong> trong>Immunodeficiency,trong> trong>Autosomaltrong> trong>Recessive,trong> T Cell-Negative, B Cell-Negative, NK Cell-Positive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease trong>Severetrong> trong>Combinedtrong> trong>Immunodeficiency,trong> trong>Autosomaltrong> trong>Recessive,trong> T Cell-Negative, B Cell-Negative, NK Cell-Positive from the curated CTD Gene-Disease Associations dataset.

trong>Severetrong> trong>Combinedtrong> trong>Immunodeficiency,trong> trong>Autosomaltrong> trong>Recessive,trong> T Cell Negative, B Cell Positive, NK Cell Positive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease trong>Severetrong> trong>Combinedtrong> trong>Immunodeficiency,trong> trong>Autosomaltrong> trong>Recessive,trong> T Cell Negative, B Cell Positive, NK Cell Positive from the curated CTD Gene-Disease Associations dataset.

trong>severetrong> trong>combinedtrong> trong>immunodeficiency,trong> t cell-negative, b-cell/natural killer-cell positive Gene Set

From OMIM Gene-Disease Associations

genes associated with the trong>severetrong> trong>combinedtrong> trong>immunodeficiency,trong> t cell-negative, b-cell/natural killer-cell positive phenotype from the curated OMIM Gene-Disease Associations dataset.

trong>severetrong> trong>combinedtrong> trong>immunodeficiency,trong> t-cell negative, b-cell/natural killer cell-positive type Gene Set

From OMIM Gene-Disease Associations

genes associated with the trong>severetrong> trong>combinedtrong> trong>immunodeficiency,trong> t-cell negative, b-cell/natural killer cell-positive type phenotype from the curated OMIM Gene-Disease Associations dataset.

Immunodeficiency 18, trong>severetrong> trong>combinedtrong> immunodeficiency variant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Immunodeficiency 18, trong>severetrong> trong>combinedtrong> immunodeficiency variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>severetrong> trong>combinedtrong> trong>immunodeficiency,trong> b cell-negative Gene Set

From OMIM Gene-Disease Associations

genes associated with the trong>severetrong> trong>combinedtrong> trong>immunodeficiency,trong> b cell-negative phenotype from the curated OMIM Gene-Disease Associations dataset.

X-linked trong>severetrong> trong>combinedtrong> immunodeficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the X-linked trong>severetrong> trong>combinedtrong> immunodeficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Severetrong> trong>combinedtrong> immunodeficiency due to ADA deficiency Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Severetrong> trong>combinedtrong> immunodeficiency due to ADA deficiency phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Severetrong> trong>combinedtrong> immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Severetrong> trong>combinedtrong> immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Severetrong> trong>combinedtrong> trong>immunodeficiency,trong> atypical Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Severetrong> trong>combinedtrong> trong>immunodeficiency,trong> atypical phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Severetrong> trong>combinedtrong> immunodeficiency disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Severetrong> trong>combinedtrong> immunodeficiency disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Severetrong> trong>combinedtrong> immunodeficiency with sensitivity to ionizing radiation Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Severetrong> trong>combinedtrong> immunodeficiency with sensitivity to ionizing radiation phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Severetrong> trong>Combinedtrong> Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease trong>Severetrong> trong>Combinedtrong> Immunodeficiency with Microcephaly, Growth Retardation, and Sensitivity to Ionizing Radiation from the curated CTD Gene-Disease Associations dataset.

trong>Severetrong> trong>Combinedtrong> Immunodeficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease trong>Severetrong> trong>Combinedtrong> Immunodeficiency from the curated CTD Gene-Disease Associations dataset.

trong>Severetrong> trong>combinedtrong> immunodeficiency due to adenosine deaminase deficiency Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease trong>Severetrong> trong>combinedtrong> immunodeficiency due to adenosine deaminase deficiency from the curated CTD Gene-Disease Associations dataset.

trong>Severetrong> trong>combinedtrong> immunodeficiency with sensitivity to ionizing radiation Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease trong>Severetrong> trong>combinedtrong> immunodeficiency with sensitivity to ionizing radiation from the curated CTD Gene-Disease Associations dataset.

trong>severetrong> trong>combinedtrong> immunodeficiency Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease trong>severetrong> trong>combinedtrong> immunodeficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

trong>severetrong> trong>combinedtrong> immunodeficiency Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease trong>severetrong> trong>combinedtrong> immunodeficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

lymphopenia; scid; trong>severetrong> trong>combinedtrong> immunodeficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease lymphopenia; scid; trong>severetrong> trong>combinedtrong> immunodeficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

x-linked trong>severetrong> trong>combinedtrong> immunodeficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease x-linked trong>severetrong> trong>combinedtrong> immunodeficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

immunologic deficiency syndromes; trong>severetrong> trong>combinedtrong> immunodeficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease immunologic deficiency syndromes; trong>severetrong> trong>combinedtrong> immunodeficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

trong>severetrong> trong>combinedtrong> immunodeficiency Gene Set

From HPO Gene-Disease Associations

genes associated with the trong>severetrong> trong>combinedtrong> immunodeficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

trong>Severetrong> trong>Combinedtrong> Immunodeficiency Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the trong>Severetrong> trong>Combinedtrong> Immunodeficiency phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

trong>severetrong> trong>combinedtrong> immunodeficiency due to il2 deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the trong>severetrong> trong>combinedtrong> immunodeficiency due to il2 deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

trong>severetrong> trong>combinedtrong> immunodeficiency due to ada deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the trong>severetrong> trong>combinedtrong> immunodeficiency due to ada deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

trong>severetrong> trong>combinedtrong> immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation Gene Set

From OMIM Gene-Disease Associations

genes associated with the trong>severetrong> trong>combinedtrong> immunodeficiency with microcephaly, growth retardation, and sensitivity to ionizing radiation phenotype from the curated OMIM Gene-Disease Associations dataset.

trong>severetrong> trong>combinedtrong> trong>immunodeficiency,trong> athabascan type Gene Set

From OMIM Gene-Disease Associations

genes associated with the trong>severetrong> trong>combinedtrong> trong>immunodeficiency,trong> athabascan type phenotype from the curated OMIM Gene-Disease Associations dataset.

trong>severetrong> trong>combinedtrong> trong>immunodeficiency,trong> x-linked Gene Set

From OMIM Gene-Disease Associations

genes associated with the trong>severetrong> trong>combinedtrong> trong>immunodeficiency,trong> x-linked phenotype from the curated OMIM Gene-Disease Associations dataset.

trong>Severetrong> trong>autosomaltrong> recessive muscular dystrophy of childhood - North African type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Severetrong> trong>autosomaltrong> recessive muscular dystrophy of childhood - North African type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Severetrong> congenital neutropenia 3, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Severetrong> congenital neutropenia 3, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Severetrong> congenital neutropenia 6, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Severetrong> congenital neutropenia 6, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Severetrong> congenital neutropenia 4, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Severetrong> congenital neutropenia 4, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neutropenia, trong>Severetrong> Congenital, trong>Autosomaltrong> Recessive 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neutropenia, trong>Severetrong> Congenital, trong>Autosomaltrong> Recessive 3 from the curated CTD Gene-Disease Associations dataset.

Neutropenia, trong>Severetrong> Congenital, trong>Autosomaltrong> Recessive 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neutropenia, trong>Severetrong> Congenital, trong>Autosomaltrong> Recessive 4 from the curated CTD Gene-Disease Associations dataset.

neutropenia, trong>severetrong> congenital 3, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the neutropenia, trong>severetrong> congenital 3, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

neutropenia, trong>severetrong> congenital, 6, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the neutropenia, trong>severetrong> congenital, 6, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

neutropenia, trong>severetrong> congenital, 5, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the neutropenia, trong>severetrong> congenital, 5, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

neutropenia, trong>severetrong> congenital 4, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the neutropenia, trong>severetrong> congenital 4, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency 32b, monocyte and dendritic cell deficiency, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency 32b, monocyte and dendritic cell deficiency, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

trong>combinedtrong> t cell and b cell immunodeficiency Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease trong>combinedtrong> t cell and b cell immunodeficiency from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

trong>combinedtrong> t cell and b cell immunodeficiency Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease trong>combinedtrong> t cell and b cell immunodeficiency in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

immunodeficiency 31b, mycobacterial and viral infections, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency 31b, mycobacterial and viral infections, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

trong>immunodeficiency,trong> primary, trong>autosomaltrong> trong>recessive,trong> il21r-related Gene Set

From OMIM Gene-Disease Associations

genes associated with the trong>immunodeficiency,trong> primary, trong>autosomaltrong> trong>recessive,trong> il21r-related phenotype from the curated OMIM Gene-Disease Associations dataset.

scid, trong>autosomaltrong> trong>recessive,trong> t-negative/b-positive type Gene Set

From OMIM Gene-Disease Associations

genes associated with the scid, trong>autosomaltrong> trong>recessive,trong> t-negative/b-positive type phenotype from the curated OMIM Gene-Disease Associations dataset.

SCID - trong>Severetrong> trong>combinedtrong> immunodeficiency_Lung Tissue_GSE3414 Gene Set

From GEO Signatures of Differentially Expressed Genes for Diseases

genes differentially expressed during SCID - trong>Severetrong> trong>combinedtrong> immunodeficiency_Lung Tissue_GSE3414 disease perturbation from the GEO Signatures of Differentially Expressed Genes for Diseases dataset.

trong>severetrong> t-cell immunodeficiency Gene Set

From HPO Gene-Disease Associations

genes associated with the trong>severetrong> t-cell immunodeficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

trong>Combinedtrong> trong>immunodeficiency,trong> X-linked Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Combinedtrong> trong>immunodeficiency,trong> X-linked phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

X-Linked trong>Combinedtrong> Immunodeficiency Diseases Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease X-Linked trong>Combinedtrong> Immunodeficiency Diseases from the curated CTD Gene-Disease Associations dataset.

trong>combinedtrong> immunodeficiency Gene Set

From HPO Gene-Disease Associations

genes associated with the trong>combinedtrong> immunodeficiency phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

trong>combinedtrong> trong>immunodeficiency,trong> x-linked, moderate Gene Set

From OMIM Gene-Disease Associations

genes associated with the trong>combinedtrong> trong>immunodeficiency,trong> x-linked, moderate phenotype from the curated OMIM Gene-Disease Associations dataset.

acquired immunodeficiency syndrome; hiv infections; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acquired immunodeficiency syndrome; hiv infections; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acquired immunodeficiency syndrome; chromosome deletion; hiv infections; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acquired immunodeficiency syndrome; chromosome deletion; hiv infections; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acquired immunodeficiency syndrome; hiv infections; pregnancy complications, infectious; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acquired immunodeficiency syndrome; hiv infections; pregnancy complications, infectious; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

acquired immunodeficiency syndrome; hiv infections; spondylarthropathies; [x]human immunodeficiency virus disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease acquired immunodeficiency syndrome; hiv infections; spondylarthropathies; [x]human immunodeficiency virus disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Granulomatous disease, chronic, trong>autosomaltrong> trong>recessive,trong> cytochrome b-negative Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Granulomatous disease, chronic, trong>autosomaltrong> trong>recessive,trong> cytochrome b-negative phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Granulomatous Disease, Chronic, trong>Autosomaltrong> trong>Recessive,trong> Cytochrome B-Negative Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Granulomatous Disease, Chronic, trong>Autosomaltrong> trong>Recessive,trong> Cytochrome B-Negative from the curated CTD Gene-Disease Associations dataset.

trong>Severetrong> congenital neutropenia trong>autosomaltrong> dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Severetrong> congenital neutropenia trong>autosomaltrong> dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Severetrong> congenital neutropenia 2, trong>autosomaltrong> dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Severetrong> congenital neutropenia 2, trong>autosomaltrong> dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neutropenia, trong>Severetrong> Congenital, trong>Autosomaltrong> Dominant 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neutropenia, trong>Severetrong> Congenital, trong>Autosomaltrong> Dominant 2 from the curated CTD Gene-Disease Associations dataset.

Hypertension, Early-Onset, trong>Autosomaltrong> Dominant, with trong>Severetrong> Exacerbation in Pregnancy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypertension, Early-Onset, trong>Autosomaltrong> Dominant, with trong>Severetrong> Exacerbation in Pregnancy from the curated CTD Gene-Disease Associations dataset.

Neutropenia, trong>Severetrong> Congenital, trong>Autosomaltrong> Dominant 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neutropenia, trong>Severetrong> Congenital, trong>Autosomaltrong> Dominant 1 from the curated CTD Gene-Disease Associations dataset.

neutropenia, trong>severetrong> congenital 1, trong>autosomaltrong> dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the neutropenia, trong>severetrong> congenital 1, trong>autosomaltrong> dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

neutropenia, trong>severetrong> congenital 2, trong>autosomaltrong> dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the neutropenia, trong>severetrong> congenital 2, trong>autosomaltrong> dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

Chronic granulomatous disease, trong>autosomaltrong> recessive cytochrome b-positive, type 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chronic granulomatous disease, trong>autosomaltrong> recessive cytochrome b-positive, type 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chronic granulomatous disease, trong>autosomaltrong> recessive cytochrome b-positive, type 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chronic granulomatous disease, trong>autosomaltrong> recessive cytochrome b-positive, type 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Chronic granulomatous disease, trong>autosomaltrong> recessive cytochrome b-positive, type 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Chronic granulomatous disease, trong>autosomaltrong> recessive cytochrome b-positive, type 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Granulomatous Disease, Chronic, trong>Autosomaltrong> trong>Recessive,trong> Cytochrome B-Positive, Type I Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Granulomatous Disease, Chronic, trong>Autosomaltrong> trong>Recessive,trong> Cytochrome B-Positive, Type I from the curated CTD Gene-Disease Associations dataset.

Granulomatous Disease, Chronic, trong>Autosomaltrong> trong>Recessive,trong> Cytochrome B-Positive, Type II Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Granulomatous Disease, Chronic, trong>Autosomaltrong> trong>Recessive,trong> Cytochrome B-Positive, Type II from the curated CTD Gene-Disease Associations dataset.

granulomatous disease, chronic, trong>autosomaltrong> trong>recessive,trong> cytochrome b-positive, type iii Gene Set

From OMIM Gene-Disease Associations

genes associated with the granulomatous disease, chronic, trong>autosomaltrong> trong>recessive,trong> cytochrome b-positive, type iii phenotype from the curated OMIM Gene-Disease Associations dataset.

Ectodermal dysplasia, anhidrotic, with T-cell trong>immunodeficiency,trong> trong>autosomaltrong> dominant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectodermal dysplasia, anhidrotic, with T-cell trong>immunodeficiency,trong> trong>autosomaltrong> dominant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectodermal Dysplasia, Anhidrotic, With T-Cell trong>Immunodeficiency,trong> trong>Autosomaltrong> Dominant Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectodermal Dysplasia, Anhidrotic, With T-Cell trong>Immunodeficiency,trong> trong>Autosomaltrong> Dominant from the curated CTD Gene-Disease Associations dataset.

trong>autosomaltrong> dominant anhidrotic ectodermal dysplasia and t cell immunodeficiency Gene Set

From GAD Gene-Disease Associations

genes associated with the disease trong>autosomaltrong> dominant anhidrotic ectodermal dysplasia and t cell immunodeficiency in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Breast cancer (estrogen-receptor negative, progesterone-receptor negative, and human epidermal growth factor-receptor negative) Gene Set

From GWAS Catalog SNP-Phenotype Associations

genes associated with the Breast cancer (estrogen-receptor negative, progesterone-receptor negative, and human epidermal growth factor-receptor negative) phenotype in GWAS datasets from the GWAS Catalog SNP-Phenotype Associations dataset.

immunodeficiency 31a, mycobacteriosis, trong>autosomaltrong> dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency 31a, mycobacteriosis, trong>autosomaltrong> dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency 31c, trong>autosomaltrong> dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency 31c, trong>autosomaltrong> dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

immunodeficiency 32a, mycobacteriosis, trong>autosomaltrong> dominant Gene Set

From OMIM Gene-Disease Associations

genes associated with the immunodeficiency 32a, mycobacteriosis, trong>autosomaltrong> dominant phenotype from the curated OMIM Gene-Disease Associations dataset.

Monocyte and dendritic cell deficiency, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Monocyte and dendritic cell deficiency, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, trong>severetrong> cytomegalovirus infection, and autoimmunity Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alpha/beta T-cell lymphopenia with gamma/delta T-cell expansion, trong>severetrong> cytomegalovirus infection, and autoimmunity phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alpha/Beta T-Cell Lymphopenia with Gamma/Delta T-Cell Expansion, trong>Severetrong> Cytomegalovirus Infection, and Autoimmunity Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Alpha/Beta T-Cell Lymphopenia with Gamma/Delta T-Cell Expansion, trong>Severetrong> Cytomegalovirus Infection, and Autoimmunity from the curated CTD Gene-Disease Associations dataset.

alpha/beta t-cell lymphopenia with gamma/delta t-cell expansion, trong>severetrong> cytomegalovirus infection, and autoimmunity Gene Set

From OMIM Gene-Disease Associations

genes associated with the alpha/beta t-cell lymphopenia with gamma/delta t-cell expansion, trong>severetrong> cytomegalovirus infection, and autoimmunity phenotype from the curated OMIM Gene-Disease Associations dataset.

negative regulation of cell-cell adhesion by negative regulation of transcription from rna polymerase ii promoter Gene Set

From GO Biological Process Annotations

genes participating in the negative regulation of cell-cell adhesion by negative regulation of transcription from rna polymerase ii promoter biological process from the curated GO Biological Process Annotations dataset.

Methionine adenosyltransferase deficiency, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Methionine adenosyltransferase deficiency, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mandibulofacial dysostosis, Treacher Collins type, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mandibulofacial dysostosis, Treacher Collins type, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ocular coloboma, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ocular coloboma, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Primary trong>autosomaltrong> recessive microcephaly 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Primary trong>autosomaltrong> recessive microcephaly 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Primary trong>autosomaltrong> recessive microcephaly 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Primary trong>autosomaltrong> recessive microcephaly 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Primary trong>autosomaltrong> recessive microcephaly 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Primary trong>autosomaltrong> recessive microcephaly 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Primary trong>autosomaltrong> recessive microcephaly 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Primary trong>autosomaltrong> recessive microcephaly 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Primary trong>autosomaltrong> recessive microcephaly 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Primary trong>autosomaltrong> recessive microcephaly 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly 12, primary, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly 12, primary, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Agammaglobulinemia 2, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Agammaglobulinemia 2, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Neuropathy, hereditary sensory, with spastic paraplegia, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Neuropathy, hereditary sensory, with spastic paraplegia, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 101 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 101 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 103 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 103 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Autosomaltrong> recessive hypophosphatemic vitamin D refractory rickets Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Autosomaltrong> recessive hypophosphatemic vitamin D refractory rickets phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia due to protein S deficiency, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombophilia due to protein S deficiency, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Autosomaltrong> recessive cutis laxa type 1B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Autosomaltrong> recessive cutis laxa type 1B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Auditory neuropathy, trong>autosomaltrong> trong>recessive,trong> 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Auditory neuropathy, trong>autosomaltrong> trong>recessive,trong> 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypercholesterolemia, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypercholesterolemia, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Woolly hair, trong>autosomaltrong> recessive 2, with or without hypotrichosis Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Woolly hair, trong>autosomaltrong> recessive 2, with or without hypotrichosis phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Exfoliative ichthyosis, trong>autosomaltrong> trong>recessive,trong> ichthyosis bullosa of siemens-like Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Exfoliative ichthyosis, trong>autosomaltrong> trong>recessive,trong> ichthyosis bullosa of siemens-like phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Alport syndrome, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Alport syndrome, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, trong>autosomaltrong> recessive 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, trong>autosomaltrong> recessive 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, trong>autosomaltrong> recessive 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, trong>autosomaltrong> recessive 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, trong>autosomaltrong> recessive 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, trong>autosomaltrong> recessive 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nemaline myopathy 3, trong>autosomaltrong> dominant or recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nemaline myopathy 3, trong>autosomaltrong> dominant or recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ectopia lentis, isolated trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ectopia lentis, isolated trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Primary hypertrophic osteoarthropathy, trong>autosomaltrong> recessive 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Primary hypertrophic osteoarthropathy, trong>autosomaltrong> recessive 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Autosomaltrong> recessive hypophosphatemic bone disease Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Autosomaltrong> recessive hypophosphatemic bone disease phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Inflammatory bowel disease 25, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Inflammatory bowel disease 25, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 30 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 30 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 37 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 37 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 35 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 35 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 39 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 39 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dystonia, dopa-responsive, with or without hyperphenylalaninemia, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dystonia, dopa-responsive, with or without hyperphenylalaninemia, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Osteopetrosis, trong>autosomaltrong> recessive 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Osteopetrosis, trong>autosomaltrong> recessive 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 46, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 46, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 48, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 48, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Tetraamelia, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Tetraamelia, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 25 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 25 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 24 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 24 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 23 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 23 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 22 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 22 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 29 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 29 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 28 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 28 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thyroid hormone resistance, generalized, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thyroid hormone resistance, generalized, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Primary trong>autosomaltrong> recessive microcephaly 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Primary trong>autosomaltrong> recessive microcephaly 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Primary trong>autosomaltrong> recessive microcephaly 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Primary trong>autosomaltrong> recessive microcephaly 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 59 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 59 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myoglobinuria, acute recurrent, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myoglobinuria, acute recurrent, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal tubular acidosis, distal, trong>autosomaltrong> trong>recessive,trong> with late-onset sensorineural hearing loss Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal tubular acidosis, distal, trong>autosomaltrong> trong>recessive,trong> with late-onset sensorineural hearing loss phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cerebral trong>autosomaltrong> recessive arteriopathy with subcortical infarcts and leukoencephalopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cerebral trong>autosomaltrong> recessive arteriopathy with subcortical infarcts and leukoencephalopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hyperimmunoglobulin E recurrent infection syndrome, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hyperimmunoglobulin E recurrent infection syndrome, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia trong>autosomaltrong> recessive 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia trong>autosomaltrong> recessive 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease 6, trong>autosomaltrong> recessive early-onset Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease 6, trong>autosomaltrong> recessive early-onset phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, trong>autosomaltrong> recessive congenital 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, trong>autosomaltrong> recessive congenital 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amyotrophic lateral sclerosis 1, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis 1, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hydrocephalus, nonsyndromic, trong>autosomaltrong> recessive 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hydrocephalus, nonsyndromic, trong>autosomaltrong> recessive 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Renal tubular acidosis, distal, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Renal tubular acidosis, distal, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 54, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 54, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ataxia, spastic, 4, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ataxia, spastic, 4, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly 10, primary, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly 10, primary, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Heterotopia, periventricular, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Heterotopia, periventricular, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Persistent hyperplastic primary vitreous, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Persistent hyperplastic primary vitreous, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epidermolysis bullosa dystrophica, trong>autosomaltrong> trong>recessive,trong> localisata variant Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epidermolysis bullosa dystrophica, trong>autosomaltrong> trong>recessive,trong> localisata variant phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 11, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 11, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ehlers-Danlos syndrome, trong>autosomaltrong> trong>recessive,trong> cardiac valvular form Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ehlers-Danlos syndrome, trong>autosomaltrong> trong>recessive,trong> cardiac valvular form phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Robinow syndrome, trong>autosomaltrong> trong>recessive,trong> with brachy-syn-polydactyly Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Robinow syndrome, trong>autosomaltrong> trong>recessive,trong> with brachy-syn-polydactyly phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 57, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 57, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia, trong>autosomaltrong> recessive 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia, trong>autosomaltrong> recessive 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 102 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 102 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 72, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 72, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Segawa syndrome, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Segawa syndrome, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Myopia 23, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Myopia 23, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Klippel-Feil syndrome 2, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Klippel-Feil syndrome 2, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Autosomaltrong> recessive hypohidrotic ectodermal dysplasia syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Autosomaltrong> recessive hypohidrotic ectodermal dysplasia syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia, trong>autosomaltrong> recessive 15 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia, trong>autosomaltrong> recessive 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia, trong>autosomaltrong> recessive 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia, trong>autosomaltrong> recessive 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia, trong>autosomaltrong> recessive 11 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia, trong>autosomaltrong> recessive 11 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia, trong>autosomaltrong> recessive 10 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia, trong>autosomaltrong> recessive 10 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 44, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 44, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic ataxia 5, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic ataxia 5, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Indifference to pain, congenital, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Indifference to pain, congenital, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Retinal degeneration, trong>autosomaltrong> trong>recessive,trong> clumped pigment type Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Retinal degeneration, trong>autosomaltrong> trong>recessive,trong> clumped pigment type phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Amyotrophic lateral sclerosis 6, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Amyotrophic lateral sclerosis 6, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epidermolysis bullosa simplex, trong>autosomaltrong> recessive 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epidermolysis bullosa simplex, trong>autosomaltrong> recessive 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 18b Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 18b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 55, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 55, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Autosomaltrong> recessive congenital ichthyosis 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Autosomaltrong> recessive congenital ichthyosis 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sick sinus syndrome 1, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sick sinus syndrome 1, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, trong>autosomaltrong> recessive 18 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, trong>autosomaltrong> recessive 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 63, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 63, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, trong>autosomaltrong> recessive 27 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, trong>autosomaltrong> recessive 27 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Nemaline myopathy 2, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Nemaline myopathy 2, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Congenital myotonia, trong>autosomaltrong> recessive form Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Congenital myotonia, trong>autosomaltrong> recessive form phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 91 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 91 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 84b Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 84b phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, congenital nuclear, trong>autosomaltrong> recessive 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, congenital nuclear, trong>autosomaltrong> recessive 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Cataract, congenital nuclear, trong>autosomaltrong> recessive 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Cataract, congenital nuclear, trong>autosomaltrong> recessive 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Polymicrogyria, bilateral perisylvian, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Polymicrogyria, bilateral perisylvian, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia trong>autosomaltrong> recessive with axonal neuropathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia trong>autosomaltrong> recessive with axonal neuropathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Autosomaltrong> recessive Dejerine-Sottas syndrome Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Autosomaltrong> recessive Dejerine-Sottas syndrome phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, trong>autosomaltrong> recessive 39 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, trong>autosomaltrong> recessive 39 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Glut1 deficiency syndrome 1, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Glut1 deficiency syndrome 1, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 86 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 86 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 81 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 81 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Oculodentodigital dysplasia, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Oculodentodigital dysplasia, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 89 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 89 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 88 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 88 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 48 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 48 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia, trong>autosomaltrong> recessive 14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia, trong>autosomaltrong> recessive 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia, trong>autosomaltrong> recessive 9 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia, trong>autosomaltrong> recessive 9 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia, trong>autosomaltrong> recessive 8 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia, trong>autosomaltrong> recessive 8 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Pseudohypoaldosteronism type 1 trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Pseudohypoaldosteronism type 1 trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, trong>autosomaltrong> recessive 38 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, trong>autosomaltrong> recessive 38 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Sclerocornea, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Sclerocornea, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 56, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 56, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, trong>autosomaltrong> recessive 34 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, trong>autosomaltrong> recessive 34 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 53 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 53 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 30, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 30, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Epidermolysis bullosa dystrophica inversa, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Epidermolysis bullosa dystrophica inversa, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly and chorioretinopathy, trong>autosomaltrong> trong>recessive,trong> 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly and chorioretinopathy, trong>autosomaltrong> trong>recessive,trong> 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Dyskeratosis congenita, trong>autosomaltrong> trong>recessive,trong> 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Dyskeratosis congenita, trong>autosomaltrong> trong>recessive,trong> 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Agammaglobulinemia 6, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Agammaglobulinemia 6, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Agammaglobulinemia 7, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Agammaglobulinemia 7, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, trong>autosomaltrong> recessive 13 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, trong>autosomaltrong> recessive 13 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, trong>autosomaltrong> recessive 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, trong>autosomaltrong> recessive 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, trong>autosomaltrong> recessive 14 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, trong>autosomaltrong> recessive 14 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Ataxia, spastic, 2, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Ataxia, spastic, 2, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spinocerebellar ataxia trong>autosomaltrong> recessive 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spinocerebellar ataxia trong>autosomaltrong> recessive 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 42 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 42 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 44 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 44 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 45, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Spastic paraplegia 45, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 31 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 31 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mycobacterial and viral infections, susceptibility to, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mycobacterial and viral infections, susceptibility to, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, trong>autosomaltrong> recessive 47 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, trong>autosomaltrong> recessive 47 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Parkinson disease, trong>autosomaltrong> recessive early-onset, digenic, PINK1/DJ1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Parkinson disease, trong>autosomaltrong> recessive early-onset, digenic, PINK1/DJ1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Osteopetrosis trong>autosomaltrong> recessive 7 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Osteopetrosis trong>autosomaltrong> recessive 7 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Osteopetrosis trong>autosomaltrong> recessive 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Osteopetrosis trong>autosomaltrong> recessive 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Osteopetrosis trong>autosomaltrong> recessive 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Osteopetrosis trong>autosomaltrong> recessive 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Osteopetrosis trong>autosomaltrong> recessive 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Osteopetrosis trong>autosomaltrong> recessive 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Osteopetrosis trong>autosomaltrong> recessive 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Osteopetrosis trong>autosomaltrong> recessive 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 76 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 76 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 77 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 77 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 74 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 74 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 70 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 70 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 79 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 79 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Autosomaltrong> recessive cutis laxa type 2B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Autosomaltrong> recessive cutis laxa type 2B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Autosomaltrong> recessive cutis laxa type IA Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Autosomaltrong> recessive cutis laxa type IA phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Autosomaltrong> recessive centronuclear myopathy Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Autosomaltrong> recessive centronuclear myopathy phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Autosomaltrong> recessive congenital ichthyosis 5 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Autosomaltrong> recessive congenital ichthyosis 5 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Autosomaltrong> recessive congenital ichthyosis 6 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Autosomaltrong> recessive congenital ichthyosis 6 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Autosomaltrong> recessive congenital ichthyosis 1 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Autosomaltrong> recessive congenital ichthyosis 1 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Autosomaltrong> recessive congenital ichthyosis 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Autosomaltrong> recessive congenital ichthyosis 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Autosomaltrong> recessive congenital ichthyosis 3 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Autosomaltrong> recessive congenital ichthyosis 3 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 18 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 18 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 61 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 61 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 63 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 63 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 67 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 67 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Thrombophilia, hereditary, due to protein C deficiency, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Thrombophilia, hereditary, due to protein C deficiency, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Autosomaltrong> recessive congenital ichthyosis 4A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Autosomaltrong> recessive congenital ichthyosis 4A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Autosomaltrong> recessive congenital ichthyosis 4B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Autosomaltrong> recessive congenital ichthyosis 4B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

trong>Autosomaltrong> recessive cutis laxa type 3B Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the trong>Autosomaltrong> recessive cutis laxa type 3B phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly 11, primary, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly 11, primary, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly with chorioretinopathy, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly with chorioretinopathy, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Robinow syndrome, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Robinow syndrome, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Gonadal dysgenesis with auditory dysfunction, trong>autosomaltrong> recessive inheritance Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Gonadal dysgenesis with auditory dysfunction, trong>autosomaltrong> recessive inheritance phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, trong>autosomaltrong> recessive 40 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, trong>autosomaltrong> recessive 40 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, trong>autosomaltrong> recessive 41 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, trong>autosomaltrong> recessive 41 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, trong>autosomaltrong> recessive 42 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, trong>autosomaltrong> recessive 42 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, trong>autosomaltrong> recessive 43 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, trong>autosomaltrong> recessive 43 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, trong>autosomaltrong> recessive 44 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, trong>autosomaltrong> recessive 44 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, trong>autosomaltrong> recessive 45 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, trong>autosomaltrong> recessive 45 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Mental retardation, trong>autosomaltrong> recessive 46 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Mental retardation, trong>autosomaltrong> recessive 46 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Bestrophinopathy, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Bestrophinopathy, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly 9, primary, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly 9, primary, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Anemia, sideroblastic, pyridoxine-refractory, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Anemia, sideroblastic, pyridoxine-refractory, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Distal spinal muscular atrophy, trong>autosomaltrong> recessive 4 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Distal spinal muscular atrophy, trong>autosomaltrong> recessive 4 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Hypophosphatemic rickets, trong>autosomaltrong> trong>recessive,trong> 2 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Hypophosphatemic rickets, trong>autosomaltrong> trong>recessive,trong> 2 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 15 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 15 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 16 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 16 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 12 Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 12 phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Microcephaly 13, primary, trong>autosomaltrong> recessive Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Microcephaly 13, primary, trong>autosomaltrong> recessive phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Deafness, trong>autosomaltrong> recessive 1A Gene Set

From ClinVar Gene-Phenotype Associations

genes associated with the Deafness, trong>autosomaltrong> recessive 1A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Spastic paraplegia 20, trong>autosomaltrong> recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic paraplegia 20, trong>autosomaltrong> recessive from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 1b Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 1b from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 32 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 32 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 1A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 1A from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 14 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 14 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 16 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 16 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 17 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 17 from the curated CTD Gene-Disease Associations dataset.

Spastic Paraplegia 32, trong>Autosomaltrong> Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic Paraplegia 32, trong>Autosomaltrong> Recessive from the curated CTD Gene-Disease Associations dataset.

Osteopetrosis, trong>Autosomaltrong> Recessive 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Osteopetrosis, trong>Autosomaltrong> Recessive 1 from the curated CTD Gene-Disease Associations dataset.

Osteopetrosis, trong>Autosomaltrong> Recessive 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Osteopetrosis, trong>Autosomaltrong> Recessive 7 from the curated CTD Gene-Disease Associations dataset.

Osteopetrosis, trong>Autosomaltrong> Recessive 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Osteopetrosis, trong>Autosomaltrong> Recessive 5 from the curated CTD Gene-Disease Associations dataset.

Osteopetrosis, trong>Autosomaltrong> Recessive 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Osteopetrosis, trong>Autosomaltrong> Recessive 4 from the curated CTD Gene-Disease Associations dataset.

DEAFNESS, AUTOSOMAL RECESSIVE 36, WITH OR WITHOUT VESTIBULAR INVOLVEMENT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease DEAFNESS, AUTOSOMAL RECESSIVE 36, WITH OR WITHOUT VESTIBULAR INVOLVEMENT from the curated CTD Gene-Disease Associations dataset.

Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, trong>Autosomaltrong> Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, trong>Autosomaltrong> Recessive from the curated CTD Gene-Disease Associations dataset.

HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease HYPERTROPHIC OSTEOARTHROPATHY, PRIMARY, AUTOSOMAL RECESSIVE, 1 from the curated CTD Gene-Disease Associations dataset.

Heterotopia, Periventricular, trong>Autosomaltrong> Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Heterotopia, Periventricular, trong>Autosomaltrong> Recessive from the curated CTD Gene-Disease Associations dataset.

OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease OSTEOPETROSIS, AUTOSOMAL RECESSIVE 2 from the curated CTD Gene-Disease Associations dataset.

Amyotrophic Lateral Sclerosis 6, trong>Autosomaltrong> Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Amyotrophic Lateral Sclerosis 6, trong>Autosomaltrong> Recessive from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 67 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 67 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 13 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 13 from the curated CTD Gene-Disease Associations dataset.

Ichthyosis with hypotrichosis, trong>autosomaltrong> recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ichthyosis with hypotrichosis, trong>autosomaltrong> recessive from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, trong>Autosomaltrong> Recessive 13 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, trong>Autosomaltrong> Recessive 13 from the curated CTD Gene-Disease Associations dataset.

DEAFNESS, AUTOSOMAL RECESSIVE 91 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease DEAFNESS, AUTOSOMAL RECESSIVE 91 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 77 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 77 from the curated CTD Gene-Disease Associations dataset.

DEAFNESS, AUTOSOMAL RECESSIVE 85 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease DEAFNESS, AUTOSOMAL RECESSIVE 85 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 79 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 79 from the curated CTD Gene-Disease Associations dataset.

Osteopetrosis, trong>Autosomaltrong> Recessive 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Osteopetrosis, trong>Autosomaltrong> Recessive 6 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 33 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 33 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 31 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 31 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 37 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 37 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 35 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 35 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 38 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 38 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 39 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 39 from the curated CTD Gene-Disease Associations dataset.

Sick Sinus Syndrome 1, trong>Autosomaltrong> Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Sick Sinus Syndrome 1, trong>Autosomaltrong> Recessive from the curated CTD Gene-Disease Associations dataset.

Mandibulofacial dysostosis, Treacher Collins type, trong>autosomaltrong> recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mandibulofacial dysostosis, Treacher Collins type, trong>autosomaltrong> recessive from the curated CTD Gene-Disease Associations dataset.

DEAFNESS, AUTOSOMAL RECESSIVE 83 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease DEAFNESS, AUTOSOMAL RECESSIVE 83 from the curated CTD Gene-Disease Associations dataset.

Ataxia, Spastic, 3, trong>Autosomaltrong> Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ataxia, Spastic, 3, trong>Autosomaltrong> Recessive from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 40 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 40 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 46 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 46 from the curated CTD Gene-Disease Associations dataset.

Candidiasis familial chronic mucocutaneous, trong>autosomaltrong> recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Candidiasis familial chronic mucocutaneous, trong>autosomaltrong> recessive from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 44 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 44 from the curated CTD Gene-Disease Associations dataset.

Spastic Paraplegia 7, trong>Autosomaltrong> Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic Paraplegia 7, trong>Autosomaltrong> Recessive from the curated CTD Gene-Disease Associations dataset.

Hypercholesterolemia, trong>Autosomaltrong> Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypercholesterolemia, trong>Autosomaltrong> Recessive from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 26 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 26 from the curated CTD Gene-Disease Associations dataset.

Indifference to Pain, Congenital, trong>Autosomaltrong> Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Indifference to Pain, Congenital, trong>Autosomaltrong> Recessive from the curated CTD Gene-Disease Associations dataset.

Robinow syndrome, trong>autosomaltrong> recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Robinow syndrome, trong>autosomaltrong> recessive from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 27 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 27 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 22 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 22 from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 25, trong>Autosomaltrong> Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 25, trong>Autosomaltrong> Recessive from the curated CTD Gene-Disease Associations dataset.

DEAFNESS, AUTOSOMAL RECESSIVE 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease DEAFNESS, AUTOSOMAL RECESSIVE 8 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 62 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 62 from the curated CTD Gene-Disease Associations dataset.

PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease PARKINSON DISEASE 14, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

Dystonia 17, Torsion, trong>Autosomaltrong> Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dystonia 17, Torsion, trong>Autosomaltrong> Recessive from the curated CTD Gene-Disease Associations dataset.

Spastic paraplegia 11, trong>autosomaltrong> recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic paraplegia 11, trong>autosomaltrong> recessive from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> trong>Recessive,trong> 24 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> trong>Recessive,trong> 24 from the curated CTD Gene-Disease Associations dataset.

CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CHARCOT-MARIE-TOOTH DISEASE, AXONAL, WITH VOCAL CORD PARESIS, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

Polycystic Kidney, trong>Autosomaltrong> Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Polycystic Kidney, trong>Autosomaltrong> Recessive from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar Ataxia, trong>Autosomaltrong> Recessive 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar Ataxia, trong>Autosomaltrong> Recessive 9 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar Ataxia, trong>Autosomaltrong> Recessive 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar Ataxia, trong>Autosomaltrong> Recessive 8 from the curated CTD Gene-Disease Associations dataset.

SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SPASTIC PARAPLEGIA 35, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

Renal tubular acidosis, distal, trong>autosomaltrong> recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Renal tubular acidosis, distal, trong>autosomaltrong> recessive from the curated CTD Gene-Disease Associations dataset.

Spastic Paraplegia 44, trong>Autosomaltrong> Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic Paraplegia 44, trong>Autosomaltrong> Recessive from the curated CTD Gene-Disease Associations dataset.

Spastic paraplegia 25, trong>autosomaltrong> recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic paraplegia 25, trong>autosomaltrong> recessive from the curated CTD Gene-Disease Associations dataset.

Myopathy, Hyaline Body, trong>Autosomaltrong> Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myopathy, Hyaline Body, trong>Autosomaltrong> Recessive from the curated CTD Gene-Disease Associations dataset.

SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SPASTIC ATAXIA 4, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

Thyroid Hormone Resistance, Generalized, trong>Autosomaltrong> Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Thyroid Hormone Resistance, Generalized, trong>Autosomaltrong> Recessive from the curated CTD Gene-Disease Associations dataset.

Cutis Laxa, trong>Autosomaltrong> trong>Recessive,trong> Type IIA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cutis Laxa, trong>Autosomaltrong> trong>Recessive,trong> Type IIA from the curated CTD Gene-Disease Associations dataset.

Cutis Laxa, trong>Autosomaltrong> trong>Recessive,trong> Type IIB Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cutis Laxa, trong>Autosomaltrong> trong>Recessive,trong> Type IIB from the curated CTD Gene-Disease Associations dataset.

Spastic paraplegia 15, trong>autosomaltrong> recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic paraplegia 15, trong>autosomaltrong> recessive from the curated CTD Gene-Disease Associations dataset.

Cerebral Palsy, Ataxic, trong>Autosomaltrong> Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cerebral Palsy, Ataxic, trong>Autosomaltrong> Recessive from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia, trong>autosomaltrong> trong>recessive,trong> with axonal neuropathy Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia, trong>autosomaltrong> trong>recessive,trong> with axonal neuropathy from the curated CTD Gene-Disease Associations dataset.

DEAFNESS, AUTOSOMAL RECESSIVE 18A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease DEAFNESS, AUTOSOMAL RECESSIVE 18A from the curated CTD Gene-Disease Associations dataset.

DEAFNESS, AUTOSOMAL RECESSIVE 74 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease DEAFNESS, AUTOSOMAL RECESSIVE 74 from the curated CTD Gene-Disease Associations dataset.

Spinal Muscular Atrophy, Distal, trong>Autosomaltrong> trong>Recessive,trong> 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, trong>Autosomaltrong> trong>Recessive,trong> 4 from the curated CTD Gene-Disease Associations dataset.

Spastic Paraplegia 39, trong>Autosomaltrong> Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic Paraplegia 39, trong>Autosomaltrong> Recessive from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 30 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 30 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 28 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 28 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 59 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 59 from the curated CTD Gene-Disease Associations dataset.

Spastic Paraplegia-50, trong>Autosomaltrong> Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic Paraplegia-50, trong>Autosomaltrong> Recessive from the curated CTD Gene-Disease Associations dataset.

SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SPASTIC PARAPLEGIA 45, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

DEAFNESS, AUTOSOMAL RECESSIVE 84A Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease DEAFNESS, AUTOSOMAL RECESSIVE 84A from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, trong>Autosomaltrong> Recessive 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, trong>Autosomaltrong> Recessive 9 from the curated CTD Gene-Disease Associations dataset.

Spastic paraplegia 14, trong>autosomaltrong> recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic paraplegia 14, trong>autosomaltrong> recessive from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, trong>Autosomaltrong> Recessive 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, trong>Autosomaltrong> Recessive 3 from the curated CTD Gene-Disease Associations dataset.

Ectodermal Dysplasia, Hypohidrotic, trong>Autosomaltrong> Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ectodermal Dysplasia, Hypohidrotic, trong>Autosomaltrong> Recessive from the curated CTD Gene-Disease Associations dataset.

AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AGAMMAGLOBULINEMIA 1, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

Anemia, Sideroblastic, Pyridoxine-Refractory, trong>Autosomaltrong> Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Anemia, Sideroblastic, Pyridoxine-Refractory, trong>Autosomaltrong> Recessive from the curated CTD Gene-Disease Associations dataset.

ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ICHTHYOSIS, CONGENITAL, AUTOSOMAL RECESSIVE 6 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, trong>Autosomaltrong> Recessive 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, trong>Autosomaltrong> Recessive 4 from the curated CTD Gene-Disease Associations dataset.

DEAFNESS, AUTOSOMAL RECESSIVE 25 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease DEAFNESS, AUTOSOMAL RECESSIVE 25 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, trong>Autosomaltrong> Recessive 11 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, trong>Autosomaltrong> Recessive 11 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, trong>Autosomaltrong> Recessive 10 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, trong>Autosomaltrong> Recessive 10 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, trong>Autosomaltrong> Recessive 8 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, trong>Autosomaltrong> Recessive 8 from the curated CTD Gene-Disease Associations dataset.

Parkinson Disease 6, trong>Autosomaltrong> Recessive Early-Onset Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinson Disease 6, trong>Autosomaltrong> Recessive Early-Onset from the curated CTD Gene-Disease Associations dataset.

Cataract, trong>Autosomaltrong> Recessive Congenital 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, trong>Autosomaltrong> Recessive Congenital 3 from the curated CTD Gene-Disease Associations dataset.

Microcephaly, Primary trong>Autosomaltrong> trong>Recessive,trong> 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microcephaly, Primary trong>Autosomaltrong> trong>Recessive,trong> 5 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia, trong>autosomaltrong> recessive 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia, trong>autosomaltrong> recessive 3 from the curated CTD Gene-Disease Associations dataset.

Hypophosphatemic Rickets, trong>Autosomaltrong> trong>Recessive,trong> 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypophosphatemic Rickets, trong>Autosomaltrong> trong>Recessive,trong> 2 from the curated CTD Gene-Disease Associations dataset.

Hypophosphatemic Rickets, trong>Autosomaltrong> trong>Recessive,trong> 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Hypophosphatemic Rickets, trong>Autosomaltrong> trong>Recessive,trong> 1 from the curated CTD Gene-Disease Associations dataset.

Microcephaly, Primary trong>Autosomaltrong> trong>Recessive,trong> 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microcephaly, Primary trong>Autosomaltrong> trong>Recessive,trong> 4 from the curated CTD Gene-Disease Associations dataset.

Microcephaly, Primary trong>Autosomaltrong> trong>Recessive,trong> 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microcephaly, Primary trong>Autosomaltrong> trong>Recessive,trong> 6 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 2 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, trong>Autosomaltrong> Recessive 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, trong>Autosomaltrong> Recessive 2 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, trong>Autosomaltrong> Recessive 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, trong>Autosomaltrong> Recessive 7 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, trong>Autosomaltrong> Recessive 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, trong>Autosomaltrong> Recessive 6 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 5 from the curated CTD Gene-Disease Associations dataset.

Cataract, trong>Autosomaltrong> trong>Recessive,trong> Early-Onset, Pulverulent Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, trong>Autosomaltrong> trong>Recessive,trong> Early-Onset, Pulverulent from the curated CTD Gene-Disease Associations dataset.

SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SPASTIC PARAPLEGIA 48, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

Microcephaly, Primary trong>Autosomaltrong> trong>Recessive,trong> 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microcephaly, Primary trong>Autosomaltrong> trong>Recessive,trong> 7 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 21 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 21 from the curated CTD Gene-Disease Associations dataset.

Colorectal Adenomatous Polyposis, trong>Autosomaltrong> Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Colorectal Adenomatous Polyposis, trong>Autosomaltrong> Recessive from the curated CTD Gene-Disease Associations dataset.

BESTROPHINOPATHY, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease BESTROPHINOPATHY, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

Inflammatory Bowel Disease 28, trong>Autosomaltrong> Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inflammatory Bowel Disease 28, trong>Autosomaltrong> Recessive from the curated CTD Gene-Disease Associations dataset.

DEAFNESS, AUTOSOMAL RECESSIVE 45 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease DEAFNESS, AUTOSOMAL RECESSIVE 45 from the curated CTD Gene-Disease Associations dataset.

Neuropathy, Hereditary Sensory, with Spastic Paraplegia, trong>Autosomaltrong> Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Neuropathy, Hereditary Sensory, with Spastic Paraplegia, trong>Autosomaltrong> Recessive from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia, trong>autosomaltrong> recessive 4 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia, trong>autosomaltrong> recessive 4 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia, trong>autosomaltrong> recessive 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia, trong>autosomaltrong> recessive 1 from the curated CTD Gene-Disease Associations dataset.

Myosclerosis, trong>Autosomaltrong> Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myosclerosis, trong>Autosomaltrong> Recessive from the curated CTD Gene-Disease Associations dataset.

Microcephaly, Primary trong>Autosomaltrong> trong>Recessive,trong> 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microcephaly, Primary trong>Autosomaltrong> trong>Recessive,trong> 3 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>autosomaltrong> recessive 51 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>autosomaltrong> recessive 51 from the curated CTD Gene-Disease Associations dataset.

Microcephaly, Primary trong>Autosomaltrong> trong>Recessive,trong> 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Microcephaly, Primary trong>Autosomaltrong> trong>Recessive,trong> 1 from the curated CTD Gene-Disease Associations dataset.

ECTOPIA LENTIS 2, ISOLATED, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease ECTOPIA LENTIS 2, ISOLATED, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia, trong>autosomaltrong> recessive 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia, trong>autosomaltrong> recessive 6 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 12 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 12 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 68 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 68 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar ataxia, trong>autosomaltrong> recessive 5 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar ataxia, trong>autosomaltrong> recessive 5 from the curated CTD Gene-Disease Associations dataset.

THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease THROMBOPHILIA DUE TO PROTEIN C DEFICIENCY, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 65 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 65 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 9 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 9 from the curated CTD Gene-Disease Associations dataset.

Dyskeratosis Congenita, trong>Autosomaltrong> Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Dyskeratosis Congenita, trong>Autosomaltrong> Recessive from the curated CTD Gene-Disease Associations dataset.

Tetra-amelia trong>autosomaltrong> recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Tetra-amelia trong>autosomaltrong> recessive from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 3 from the curated CTD Gene-Disease Associations dataset.

Mental Retardation, trong>Autosomaltrong> Recessive 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Mental Retardation, trong>Autosomaltrong> Recessive 1 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 53 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 53 from the curated CTD Gene-Disease Associations dataset.

Spinocerebellar Ataxia, trong>Autosomaltrong> Recessive 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinocerebellar Ataxia, trong>Autosomaltrong> Recessive 2 from the curated CTD Gene-Disease Associations dataset.

Epidermolysis Bullosa Simplex, trong>Autosomaltrong> Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Epidermolysis Bullosa Simplex, trong>Autosomaltrong> Recessive from the curated CTD Gene-Disease Associations dataset.

SPONDYLOCOSTAL DYSOSTOSIS 3, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SPONDYLOCOSTAL DYSOSTOSIS 3, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

AGAMMAGLOBULINEMIA 4, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AGAMMAGLOBULINEMIA 4, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease DEAFNESS, AUTOSOMAL RECESSIVE 4, WITH ENLARGED VESTIBULAR AQUEDUCT from the curated CTD Gene-Disease Associations dataset.

Myoglobinuria, Acute Recurrent, trong>Autosomaltrong> Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Myoglobinuria, Acute Recurrent, trong>Autosomaltrong> Recessive from the curated CTD Gene-Disease Associations dataset.

SPONDYLOCOSTAL DYSOSTOSIS 1, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SPONDYLOCOSTAL DYSOSTOSIS 1, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 47 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 47 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 49 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 49 from the curated CTD Gene-Disease Associations dataset.

Spinal Muscular Atrophy, Distal, trong>Autosomaltrong> trong>Recessive,trong> 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spinal Muscular Atrophy, Distal, trong>Autosomaltrong> trong>Recessive,trong> 3 from the curated CTD Gene-Disease Associations dataset.

AGAMMAGLOBULINEMIA 6, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease AGAMMAGLOBULINEMIA 6, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

Spastic Paraplegia 27, trong>Autosomaltrong> Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic Paraplegia 27, trong>Autosomaltrong> Recessive from the curated CTD Gene-Disease Associations dataset.

Cataract, Congenital Nuclear, trong>Autosomaltrong> Recessive 1 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Congenital Nuclear, trong>Autosomaltrong> Recessive 1 from the curated CTD Gene-Disease Associations dataset.

SPONDYLOCOSTAL DYSOSTOSIS 2, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SPONDYLOCOSTAL DYSOSTOSIS 2, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease CUTIS LAXA, AUTOSOMAL RECESSIVE, TYPE IA from the curated CTD Gene-Disease Associations dataset.

Oculodentodigital Dysplasia, trong>Autosomaltrong> Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Oculodentodigital Dysplasia, trong>Autosomaltrong> Recessive from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 42 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 42 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 71 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 71 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>autosomaltrong> recessive 55 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>autosomaltrong> recessive 55 from the curated CTD Gene-Disease Associations dataset.

Ehlers-Danlos Syndrome, Type VII, trong>Autosomaltrong> Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Ehlers-Danlos Syndrome, Type VII, trong>Autosomaltrong> Recessive from the curated CTD Gene-Disease Associations dataset.

Cataract, Congenital Nuclear, trong>Autosomaltrong> Recessive 3 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Congenital Nuclear, trong>Autosomaltrong> Recessive 3 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 20 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 20 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 23 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 23 from the curated CTD Gene-Disease Associations dataset.

Inclusion body myopathy trong>autosomaltrong> recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Inclusion body myopathy trong>autosomaltrong> recessive from the curated CTD Gene-Disease Associations dataset.

Cataract, Congenital Nuclear, trong>Autosomaltrong> Recessive 2 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Cataract, Congenital Nuclear, trong>Autosomaltrong> Recessive 2 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 6 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 6 from the curated CTD Gene-Disease Associations dataset.

Segawa syndrome, trong>autosomaltrong> recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Segawa syndrome, trong>autosomaltrong> recessive from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 63 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 63 from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 66 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 66 from the curated CTD Gene-Disease Associations dataset.

Spastic Paraplegia 18, trong>Autosomaltrong> Recessive Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Spastic Paraplegia 18, trong>Autosomaltrong> Recessive from the curated CTD Gene-Disease Associations dataset.

Deafness, trong>Autosomaltrong> Recessive 7 Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Deafness, trong>Autosomaltrong> Recessive 7 from the curated CTD Gene-Disease Associations dataset.

Parkinson Disease 7, trong>Autosomaltrong> Recessive Early-Onset Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease Parkinson Disease 7, trong>Autosomaltrong> Recessive Early-Onset from the curated CTD Gene-Disease Associations dataset.

SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE Gene Set

From CTD Gene-Disease Associations

genes/proteins associated with the disease SPONDYLOCOSTAL DYSOSTOSIS 4, AUTOSOMAL RECESSIVE from the curated CTD Gene-Disease Associations dataset.

trong>autosomaltrong> recessive disease Gene Set

From DISEASES Curated Gene-Disease Assocation Evidence Scores

genes involed in the disease trong>autosomaltrong> recessive disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

trong>autosomaltrong> recessive disease Gene Set

From DISEASES Experimental Gene-Disease Assocation Evidence Scores

genes associated with the disease trong>autosomaltrong> recessive disease in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

trong>autosomaltrong> recessive nonsyndromic deafness Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease trong>autosomaltrong> recessive nonsyndromic deafness in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

trong>autosomaltrong> recessive disease Gene Set

From DISEASES Text-mining Gene-Disease Assocation Evidence Scores

genes co-occuring with the disease trong>autosomaltrong> recessive disease in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

trong>autosomaltrong> recessive charcot-marie-tooth disease Gene Set

From GAD Gene-Disease Associations

genes associated with the disease trong>autosomaltrong> recessive charcot-marie-tooth disease in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

trong>autosomaltrong> recessive disease Gene Set

From GWASdb SNP-Disease Associations

genes associated with the disease trong>autosomaltrong> recessive disease in GWAS and other genetic association datasets from the GWASdb SNP-Disease Associations dataset.

trong>autosomaltrong> recessive inheritance Gene Set

From HPO Gene-Disease Associations

genes associated with the trong>autosomaltrong> recessive inheritance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Polycystic Kidney, trong>Autosomaltrong> Recessive Gene Set

From HuGE Navigator Gene-Phenotype Associations

genes associated with the Polycystic Kidney, trong>Autosomaltrong> Recessive phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

mental retardation, trong>autosomaltrong> trong>recessive,trong> 9/26 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> trong>recessive,trong> 9/26 phenotype from the curated OMIM Gene-Disease Associations dataset.

exfoliative ichthyosis, trong>autosomaltrong> trong>recessive,trong> ichthyosis bullosa of siemens-like Gene Set

From OMIM Gene-Disease Associations

genes associated with the exfoliative ichthyosis, trong>autosomaltrong> trong>recessive,trong> ichthyosis bullosa of siemens-like phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> recessive 28 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> recessive 28 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> recessive 29 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> recessive 29 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> recessive 23 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> recessive 23 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> recessive 27 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> recessive 27 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> recessive 24 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> recessive 24 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> recessive 25 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> recessive 25 phenotype from the curated OMIM Gene-Disease Associations dataset.

spondylocostal dysostosis 1, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondylocostal dysostosis 1, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 5a, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 5a, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, distal, trong>autosomaltrong> trong>recessive,trong> 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, distal, trong>autosomaltrong> trong>recessive,trong> 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, distal, trong>autosomaltrong> trong>recessive,trong> 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, distal, trong>autosomaltrong> trong>recessive,trong> 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 74 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 74 phenotype from the curated OMIM Gene-Disease Associations dataset.

spondylocostal dysostosis 2, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondylocostal dysostosis 2, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

?spinocerebellar ataxia, trong>autosomaltrong> recessive 15 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?spinocerebellar ataxia, trong>autosomaltrong> recessive 15 phenotype from the curated OMIM Gene-Disease Associations dataset.

?spinocerebellar ataxia, trong>autosomaltrong> recessive 17 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?spinocerebellar ataxia, trong>autosomaltrong> recessive 17 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 18a Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 18a phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 18b Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 18b phenotype from the curated OMIM Gene-Disease Associations dataset.

epidermolysis bullosa, nonspecific, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the epidermolysis bullosa, nonspecific, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to protein s deficiency, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to protein s deficiency, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 11b, hypohidrotic/hair/tooth type, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

?microcephaly 11, primary, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?microcephaly 11, primary, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 18, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 18, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> recessive 40 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> recessive 40 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> recessive 44 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> recessive 44 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> recessive 46 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> recessive 46 phenotype from the curated OMIM Gene-Disease Associations dataset.

osteopetrosis, trong>autosomaltrong> recessive 3, with renal tubular acidosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteopetrosis, trong>autosomaltrong> recessive 3, with renal tubular acidosis phenotype from the curated OMIM Gene-Disease Associations dataset.

hydrocephalus, nonsyndromic, trong>autosomaltrong> recessive 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hydrocephalus, nonsyndromic, trong>autosomaltrong> recessive 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 32, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 32, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 51 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 51 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 53 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 53 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 55 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 55 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 59 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 59 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly 2, primary, trong>autosomaltrong> trong>recessive,trong> with or without cortical malformations Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly 2, primary, trong>autosomaltrong> trong>recessive,trong> with or without cortical malformations phenotype from the curated OMIM Gene-Disease Associations dataset.

neuromyotonia and axonal neuropathy, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the neuromyotonia and axonal neuropathy, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 53, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 53, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

ectopia lentis, isolated, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectopia lentis, isolated, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

heterotaxy, visceral, 6, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the heterotaxy, visceral, 6, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 22, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 22, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly 5, primary, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly 5, primary, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 4, with enlarged vestibular aqueduct Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 4, with enlarged vestibular aqueduct phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic ataxia 2, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic ataxia 2, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic ataxia 3, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic ataxia 3, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 76 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 76 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 77 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 77 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 70 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 70 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 71 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 71 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 79 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 79 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa, juvenile, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa, juvenile, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

protoporphyria, erythropoietic, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the protoporphyria, erythropoietic, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 1a Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 1a phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 1b Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 1b phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 15 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 15 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 16 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 16 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 17 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 17 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

thrombophilia due to protein c deficiency, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the thrombophilia due to protein c deficiency, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 30, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 30, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 85 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 85 phenotype from the curated OMIM Gene-Disease Associations dataset.

myopia 23, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopia 23, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

?spastic paraplegia 43, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?spastic paraplegia 43, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> recessive 32 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> recessive 32 phenotype from the curated OMIM Gene-Disease Associations dataset.

hydrocephalus, nonsyndromic, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the hydrocephalus, nonsyndromic, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 45, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 45, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 33 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 33 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 30 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 30 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 31 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 31 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 36 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 36 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 37 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 37 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 35 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 35 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 38 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 38 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 39 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 39 phenotype from the curated OMIM Gene-Disease Associations dataset.

ehlers-danlos syndrome, trong>autosomaltrong> trong>recessive,trong> due to tenascin x deficiency Gene Set

From OMIM Gene-Disease Associations

genes associated with the ehlers-danlos syndrome, trong>autosomaltrong> trong>recessive,trong> due to tenascin x deficiency phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 25, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 25, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

?deafness, trong>autosomaltrong> recessive 91 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?deafness, trong>autosomaltrong> recessive 91 phenotype from the curated OMIM Gene-Disease Associations dataset.

inclusion body myopathy, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the inclusion body myopathy, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 39, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 39, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> trong>recessive,trong> 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> trong>recessive,trong> 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> trong>recessive,trong> 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> trong>recessive,trong> 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> trong>recessive,trong> 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> trong>recessive,trong> 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

night blindness, congenital stationary (complete), 1f, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary (complete), 1f, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia, trong>autosomaltrong> recessive 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia, trong>autosomaltrong> recessive 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia, trong>autosomaltrong> recessive 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia, trong>autosomaltrong> recessive 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia, trong>autosomaltrong> recessive 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia, trong>autosomaltrong> recessive 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia, trong>autosomaltrong> recessive 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia, trong>autosomaltrong> recessive 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 55, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 55, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spinal muscular atrophy, chronic distal, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinal muscular atrophy, chronic distal, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> recessive 30 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> recessive 30 phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 24, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 24, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 28, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 28, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

nemaline myopathy 1, trong>autosomaltrong> dominant or recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the nemaline myopathy 1, trong>autosomaltrong> dominant or recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

{dyskeratosis congenita, trong>autosomaltrong> recessive 4} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {dyskeratosis congenita, trong>autosomaltrong> recessive 4} phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly 9, primary, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly 9, primary, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> recessive 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> recessive 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> recessive 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> recessive 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> recessive 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> recessive 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

hypercholesterolemia, familial, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypercholesterolemia, familial, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

nemaline myopathy 8, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the nemaline myopathy 8, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 11, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 11, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocrebellar ataxia, trong>autosomaltrong> recessive 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocrebellar ataxia, trong>autosomaltrong> recessive 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

inflammatory bowel disease 25, early onset, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the inflammatory bowel disease 25, early onset, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

methionine adenosyltransferase deficiency, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the methionine adenosyltransferase deficiency, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

?coloboma, ocular, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?coloboma, ocular, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 84a Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 84a phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 84b Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 84b phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 96 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 96 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 93 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 93 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 98 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 98 phenotype from the curated OMIM Gene-Disease Associations dataset.

amyotrophic lateral sclerosis 6, trong>autosomaltrong> trong>recessive,trong> with or without frontotemporal dementia Gene Set

From OMIM Gene-Disease Associations

genes associated with the amyotrophic lateral sclerosis 6, trong>autosomaltrong> trong>recessive,trong> with or without frontotemporal dementia phenotype from the curated OMIM Gene-Disease Associations dataset.

hypertrophic osteoarthropathy, primary, trong>autosomaltrong> recessive 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypertrophic osteoarthropathy, primary, trong>autosomaltrong> recessive 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

hypertrophic osteoarthropathy, primary, trong>autosomaltrong> recessive 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypertrophic osteoarthropathy, primary, trong>autosomaltrong> recessive 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> recessive 10/20 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> recessive 10/20 phenotype from the curated OMIM Gene-Disease Associations dataset.

alport syndrome, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the alport syndrome, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

dyskeratosis congenita, trong>autosomaltrong> recessive 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the dyskeratosis congenita, trong>autosomaltrong> recessive 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

dyskeratosis congenita, trong>autosomaltrong> recessive 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the dyskeratosis congenita, trong>autosomaltrong> recessive 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

dyskeratosis congenita, trong>autosomaltrong> recessive 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the dyskeratosis congenita, trong>autosomaltrong> recessive 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

dyskeratosis congenita, trong>autosomaltrong> recessive 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the dyskeratosis congenita, trong>autosomaltrong> recessive 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 8/10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 8/10 phenotype from the curated OMIM Gene-Disease Associations dataset.

bestrophinopathy, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the bestrophinopathy, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 46, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 46, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

{epidermolysis bullosa dystrophica, trong>autosomaltrong> trong>recessive,trong> modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {epidermolysis bullosa dystrophica, trong>autosomaltrong> trong>recessive,trong> modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

night blindness, congenital stationary (complete), 1b, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary (complete), 1b, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 26, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 26, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 51, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 51, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

night blindness, congenital stationary (complete), 1c, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary (complete), 1c, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly 6, primary, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly 6, primary, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

craniometaphyseal dysplasia, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the craniometaphyseal dysplasia, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

hsan2d, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the hsan2d, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

cutis laxa, trong>autosomaltrong> trong>recessive,trong> type ia Gene Set

From OMIM Gene-Disease Associations

genes associated with the cutis laxa, trong>autosomaltrong> trong>recessive,trong> type ia phenotype from the curated OMIM Gene-Disease Associations dataset.

cutis laxa, trong>autosomaltrong> trong>recessive,trong> type ib Gene Set

From OMIM Gene-Disease Associations

genes associated with the cutis laxa, trong>autosomaltrong> trong>recessive,trong> type ib phenotype from the curated OMIM Gene-Disease Associations dataset.

colorectal adenomatous polyposis, trong>autosomaltrong> trong>recessive,trong> with pilomatricomas Gene Set

From OMIM Gene-Disease Associations

genes associated with the colorectal adenomatous polyposis, trong>autosomaltrong> trong>recessive,trong> with pilomatricomas phenotype from the curated OMIM Gene-Disease Associations dataset.

?deafness, trong>autosomaltrong> recessive 103 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?deafness, trong>autosomaltrong> recessive 103 phenotype from the curated OMIM Gene-Disease Associations dataset.

?deafness, trong>autosomaltrong> recessive 102 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?deafness, trong>autosomaltrong> recessive 102 phenotype from the curated OMIM Gene-Disease Associations dataset.

?deafness, trong>autosomaltrong> recessive 101 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?deafness, trong>autosomaltrong> recessive 101 phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 47, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 47, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

hypoparathyroidism, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypoparathyroidism, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly 1, primary, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly 1, primary, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa-12, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa-12, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

?microcephaly 8, primary, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?microcephaly 8, primary, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia, trong>autosomaltrong> recessive 16 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia, trong>autosomaltrong> recessive 16 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia, trong>autosomaltrong> recessive 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia, trong>autosomaltrong> recessive 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia, trong>autosomaltrong> recessive 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia, trong>autosomaltrong> recessive 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia, trong>autosomaltrong> recessive 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia, trong>autosomaltrong> recessive 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia, trong>autosomaltrong> recessive 10 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia, trong>autosomaltrong> recessive 10 phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis, congenital, trong>autosomaltrong> recessive 4a Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis, congenital, trong>autosomaltrong> recessive 4a phenotype from the curated OMIM Gene-Disease Associations dataset.

woolly hair, trong>autosomaltrong> recessive 1, with or without hypotrichosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the woolly hair, trong>autosomaltrong> recessive 1, with or without hypotrichosis phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 32 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 32 phenotype from the curated OMIM Gene-Disease Associations dataset.

night blindness, congenital stationary (incomplete), 2b, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary (incomplete), 2b, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis, trong>autosomaltrong> recessive 4b (harlequin) Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis, trong>autosomaltrong> recessive 4b (harlequin) phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperekplexia, hereditary 1, trong>autosomaltrong> dominant or recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperekplexia, hereditary 1, trong>autosomaltrong> dominant or recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

cutis laxa, trong>autosomaltrong> trong>recessive,trong> type iiia Gene Set

From OMIM Gene-Disease Associations

genes associated with the cutis laxa, trong>autosomaltrong> trong>recessive,trong> type iiia phenotype from the curated OMIM Gene-Disease Associations dataset.

cutis laxa, trong>autosomaltrong> trong>recessive,trong> type iiib Gene Set

From OMIM Gene-Disease Associations

genes associated with the cutis laxa, trong>autosomaltrong> trong>recessive,trong> type iiib phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, trong>autosomaltrong> recessive 45 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, trong>autosomaltrong> recessive 45 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, trong>autosomaltrong> recessive 42 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, trong>autosomaltrong> recessive 42 phenotype from the curated OMIM Gene-Disease Associations dataset.

?mental retardation, trong>autosomaltrong> recessive 43 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?mental retardation, trong>autosomaltrong> recessive 43 phenotype from the curated OMIM Gene-Disease Associations dataset.

retinitis pigmentosa 4, trong>autosomaltrong> dominant or recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinitis pigmentosa 4, trong>autosomaltrong> dominant or recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 27, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 27, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

parkinson disease 15, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the parkinson disease 15, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

?anemia, sideroblastic, pyridoxine-refractory, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?anemia, sideroblastic, pyridoxine-refractory, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

{deafness, trong>autosomaltrong> recessive 12, modifier of} Gene Set

From OMIM Gene-Disease Associations

genes associated with the {deafness, trong>autosomaltrong> recessive 12, modifier of} phenotype from the curated OMIM Gene-Disease Associations dataset.

myopathy, centronuclear, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the myopathy, centronuclear, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> recessive 39 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> recessive 39 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> recessive 38 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> recessive 38 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> recessive 31 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> recessive 31 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> recessive 33 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> recessive 33 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> recessive 35 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> recessive 35 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> recessive 34 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> recessive 34 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> recessive 36 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> recessive 36 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, neurosensory, trong>autosomaltrong> recessive 47 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, neurosensory, trong>autosomaltrong> recessive 47 phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 52, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 52, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

candidiasis, familial, 5, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the candidiasis, familial, 5, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> recessive 13 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> recessive 13 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> recessive 12 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> recessive 12 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> recessive 16 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> recessive 16 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> recessive 15 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> recessive 15 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> recessive 14 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> recessive 14 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> recessive 19 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> recessive 19 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> recessive 18 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> recessive 18 phenotype from the curated OMIM Gene-Disease Associations dataset.

candidiasis, familial, 4, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the candidiasis, familial, 4, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

hyper-ige recurrent infection syndrome, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyper-ige recurrent infection syndrome, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

inflammatory bowel disease 28, early onset, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the inflammatory bowel disease 28, early onset, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 14, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 14, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

night blindness, congenital stationary (complete), 1e, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary (complete), 1e, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 56, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 56, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spinocerebellar ataxia, trong>autosomaltrong> recessive 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the spinocerebellar ataxia, trong>autosomaltrong> recessive 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly 3, primary, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly 3, primary, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

hypophosphatemic rickets, trong>autosomaltrong> trong>recessive,trong> 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the hypophosphatemic rickets, trong>autosomaltrong> trong>recessive,trong> 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

cutis laxa, trong>autosomaltrong> trong>recessive,trong> type ic Gene Set

From OMIM Gene-Disease Associations

genes associated with the cutis laxa, trong>autosomaltrong> trong>recessive,trong> type ic phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 35, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 35, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 42 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 42 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 40 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 40 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 46 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 46 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 45 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 45 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 44 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 44 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 48 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 48 phenotype from the curated OMIM Gene-Disease Associations dataset.

corneal endothelial dystrophy 2, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the corneal endothelial dystrophy 2, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

?deafness, trong>autosomaltrong> recessive 44 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?deafness, trong>autosomaltrong> recessive 44 phenotype from the curated OMIM Gene-Disease Associations dataset.

nemaline myopathy 7, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the nemaline myopathy 7, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

cutis laxa, trong>autosomaltrong> trong>recessive,trong> type iia Gene Set

From OMIM Gene-Disease Associations

genes associated with the cutis laxa, trong>autosomaltrong> trong>recessive,trong> type iia phenotype from the curated OMIM Gene-Disease Associations dataset.

cutis laxa, trong>autosomaltrong> trong>recessive,trong> type iib Gene Set

From OMIM Gene-Disease Associations

genes associated with the cutis laxa, trong>autosomaltrong> trong>recessive,trong> type iib phenotype from the curated OMIM Gene-Disease Associations dataset.

hyperekplexia 2, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the hyperekplexia 2, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

renal tubular acidosis, distal, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the renal tubular acidosis, distal, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 68 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 68 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 61 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 61 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 63 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 63 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 62 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 62 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 65 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 65 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 67 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 67 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 66 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 66 phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis, congenital, trong>autosomaltrong> recessive 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis, congenital, trong>autosomaltrong> recessive 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis, congenital, trong>autosomaltrong> recessive 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis, congenital, trong>autosomaltrong> recessive 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis, congenital, trong>autosomaltrong> recessive 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis, congenital, trong>autosomaltrong> recessive 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis, congenital, trong>autosomaltrong> recessive 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis, congenital, trong>autosomaltrong> recessive 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis, congenital, trong>autosomaltrong> recessive 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis, congenital, trong>autosomaltrong> recessive 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis, congenital, trong>autosomaltrong> recessive 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis, congenital, trong>autosomaltrong> recessive 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis, congenital, trong>autosomaltrong> recessive 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis, congenital, trong>autosomaltrong> recessive 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

ichthyosis, congenital, trong>autosomaltrong> recessive 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ichthyosis, congenital, trong>autosomaltrong> recessive 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

nemaline myopathy 3, trong>autosomaltrong> dominant or recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the nemaline myopathy 3, trong>autosomaltrong> dominant or recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

night blindness, congenital stationary (complete), 1d, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the night blindness, congenital stationary (complete), 1d, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 50, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 50, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

?deafness, trong>autosomaltrong> recessive 88 Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?deafness, trong>autosomaltrong> recessive 88 phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 44, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 44, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 15, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 15, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 9 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 9 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 3 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 3 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness , trong>autosomaltrong> recessive 86 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness , trong>autosomaltrong> recessive 86 phenotype from the curated OMIM Gene-Disease Associations dataset.

anemia, sideroblastic, pyridoxine-refractory, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the anemia, sideroblastic, pyridoxine-refractory, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> recessive 41 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> recessive 41 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 25 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 25 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 24 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 24 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 27 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 27 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 26 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 26 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 21 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 21 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 20 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 20 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 23 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 23 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 22 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 22 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 29 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 29 phenotype from the curated OMIM Gene-Disease Associations dataset.

deafness, trong>autosomaltrong> recessive 28 Gene Set

From OMIM Gene-Disease Associations

genes associated with the deafness, trong>autosomaltrong> recessive 28 phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> trong>recessive,trong> 11 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> trong>recessive,trong> 11 phenotype from the curated OMIM Gene-Disease Associations dataset.

myoglobinuria, acute recurrent, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the myoglobinuria, acute recurrent, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

mental retardation, trong>autosomaltrong> recessive 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the mental retardation, trong>autosomaltrong> recessive 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

cataract 18, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the cataract 18, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

thyroid hormone resistance, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the thyroid hormone resistance, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

tetra-amelia, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the tetra-amelia, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

factor xi deficiency, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the factor xi deficiency, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

robinow syndrome, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the robinow syndrome, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

retinal degeneration, trong>autosomaltrong> trong>recessive,trong> clumped pigment type Gene Set

From OMIM Gene-Disease Associations

genes associated with the retinal degeneration, trong>autosomaltrong> trong>recessive,trong> clumped pigment type phenotype from the curated OMIM Gene-Disease Associations dataset.

?spastic paraplegia 72, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the ?spastic paraplegia 72, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 49, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 49, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

microcephaly 4, primary, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the microcephaly 4, primary, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

parkinson disease 7, trong>autosomaltrong> recessive early-onset Gene Set

From OMIM Gene-Disease Associations

genes associated with the parkinson disease 7, trong>autosomaltrong> recessive early-onset phenotype from the curated OMIM Gene-Disease Associations dataset.

osteopetrosis, trong>autosomaltrong> recessive 2 Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteopetrosis, trong>autosomaltrong> recessive 2 phenotype from the curated OMIM Gene-Disease Associations dataset.

osteopetrosis, trong>autosomaltrong> recessive 1 Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteopetrosis, trong>autosomaltrong> recessive 1 phenotype from the curated OMIM Gene-Disease Associations dataset.

osteopetrosis, trong>autosomaltrong> recessive 7 Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteopetrosis, trong>autosomaltrong> recessive 7 phenotype from the curated OMIM Gene-Disease Associations dataset.

osteopetrosis, trong>autosomaltrong> recessive 6 Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteopetrosis, trong>autosomaltrong> recessive 6 phenotype from the curated OMIM Gene-Disease Associations dataset.

osteopetrosis, trong>autosomaltrong> recessive 5 Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteopetrosis, trong>autosomaltrong> recessive 5 phenotype from the curated OMIM Gene-Disease Associations dataset.

osteopetrosis, trong>autosomaltrong> recessive 4 Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteopetrosis, trong>autosomaltrong> recessive 4 phenotype from the curated OMIM Gene-Disease Associations dataset.

osteopetrosis, trong>autosomaltrong> recessive 8 Gene Set

From OMIM Gene-Disease Associations

genes associated with the osteopetrosis, trong>autosomaltrong> recessive 8 phenotype from the curated OMIM Gene-Disease Associations dataset.

woolly hair, trong>autosomaltrong> recessive 2 with or without hypotrichosis Gene Set

From OMIM Gene-Disease Associations

genes associated with the woolly hair, trong>autosomaltrong> recessive 2 with or without hypotrichosis phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 7, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 7, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spondylocostal dysostosis 4, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spondylocostal dysostosis 4, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.

spastic paraplegia 54, trong>autosomaltrong> recessive Gene Set

From OMIM Gene-Disease Associations

genes associated with the spastic paraplegia 54, trong>autosomaltrong> recessive phenotype from the curated OMIM Gene-Disease Associations dataset.